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Wnt10a/beta-catenin (show CTNNB1 Proteins) signaling pathway is able to exacerbate keloid cell proliferation and inhibit the apoptosis of keloid cells through its interaction with TERT (show TERT Proteins).
WNT10A plays an important role in the pathogenesis of IPF via TGF-beta (show TGFB1 Proteins) activation and it may also be a sensitive predictor for the onset of an AE-IPF.
Wnt10a regulates proliferation and apoptosis of embryonic palatal mesenchymal cells at least partially through the canonical Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling pathway.
Data indicate that that Wnt10a regulates Dspp (show DSPP Proteins) expression in mesenchymal cells.
Histone methyltransferase G9a (show EHMT2 Proteins) represses adipogenesis by inhibiting PPARgamma (show PPARG Proteins) expression and facilitating Wnt10a expression.
Mechanisms downstream of beta-catenin (show CTNNB1 Proteins) are required for Wnt6 (show WNT6 Proteins), Wnt10a and Wnt10b (show WNT10B Proteins) to influence differentiation of mesenchymal precursors.
WNT10A may be a novel angio/stromagenic growth factor
miR (show MLXIP Proteins)-378a-3p suppresses hepatic stellate cell activation, at least in part, via targeting of Wnt10a, supporting its potential utility as a novel therapeutic target for liver fibrosis.
risk of hypodontia may be related to the WNT10A polymorphism. Our results also confirm the importance of the Wnt (show WNT2 Proteins) pathway in tooth development.
WNT10A promotes the proliferation of DPCs and negatively regulates their odontoblastic differentiation.
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness
p.Arg113Cys, p.Phe228Ile, newly identified p.Arg171Leu may represent aetiological mutations underlying MLIA w/associated dental anomalies, implicating coding variants in WNT10A gene
this study demonstrated that common variations in WNT10A have pleiotropic effects on the morphology of ectodermal appendages.
WNT10A may induce kidney fibrosis and associate with kidney dysfunction in acute interstitial nephritis.
High WNT10A expression promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
Patients with bi-allelic WNT10A mutations have severe tooth agenesis.
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is strongly expressed in the cell lines of promyelocytic leukemia and Burkitt's lymphoma. In addition, it and another family member, the WNT6 gene, are strongly coexpressed in colorectal cancer cell lines. The gene overexpression may play key roles in carcinogenesis through activation of the WNT-beta-catenin-TCF signaling pathway. This gene and the WNT6 gene are clustered in the chromosome 2q35 region.
wingless-type MMTV integration site family, member 10A
, Wnt signaling ligand
, Wnt10a protein
, hypothetical protein
, WNT10A protein
, protein Wnt-10a-like
, protein Wnt-10a
, wingless related MMTV integration site 10a